GB1173191A - Process for Preparing Liquid Epoxy Oligomers - Google Patents
Process for Preparing Liquid Epoxy OligomersInfo
- Publication number
- GB1173191A GB1173191A GB14767A GB14767A GB1173191A GB 1173191 A GB1173191 A GB 1173191A GB 14767 A GB14767 A GB 14767A GB 14767 A GB14767 A GB 14767A GB 1173191 A GB1173191 A GB 1173191A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkali
- diol
- moles
- epihalohydrin
- per mole
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
- C07D303/24—Ethers with hydroxy compounds containing no oxirane rings with polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
- C08G59/06—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
- C08G59/063—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols with epihalohydrins
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Epoxy Resins (AREA)
- Epoxy Compounds (AREA)
Abstract
1,173,191. Glycidyl ethers. MœANYAGI PARI KUTATO INTEZET. 2 Jan., 1967 [31 Dec., 1965], No. 147/67. Heading C3B. Low M.W. polyglycidyl ethers having a viscosity not exceeding 20,000 C.P. at 20‹ C. are prepared by a two-stage condensation of a diol and an epihalohydrin in the presence of 2.35-3.95 moles of alkali per mole of diol: (1) at least 4.5 moles of epihalohydrin per mole of diol are reacted in the presence of up to 65% of the alkali to be used, after reaction excess epichlorohydrin is removed and then (2) the remainder of the alkali is added and condensation completed in the absence of any excess of epihalohydrin. The resultant resin is separated from the aqueous layer and deionized by treatment with a solvent, e.g. toluene and subsequently washed with water. In examples, bisphenol-A is condensed with 8 and 15 moles (respectively) of epichlorohydrin. A suitable alkali is NaOH which may be used as a 10-35% aqueous solution.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU33265 | 1965-12-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1173191A true GB1173191A (en) | 1969-12-03 |
Family
ID=32865966
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14767A Expired GB1173191A (en) | 1965-12-31 | 1967-01-02 | Process for Preparing Liquid Epoxy Oligomers |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1173191A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2137629A (en) * | 1983-04-07 | 1984-10-10 | Dow Chemical Co | A process for reducing the hydrolyzable chloride content of an epoxidation process |
EP0205214A2 (en) * | 1985-06-06 | 1986-12-17 | Shell Internationale Researchmaatschappij B.V. | Epoxy resin preparation process |
-
1967
- 1967-01-02 GB GB14767A patent/GB1173191A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2137629A (en) * | 1983-04-07 | 1984-10-10 | Dow Chemical Co | A process for reducing the hydrolyzable chloride content of an epoxidation process |
EP0205214A2 (en) * | 1985-06-06 | 1986-12-17 | Shell Internationale Researchmaatschappij B.V. | Epoxy resin preparation process |
EP0205214A3 (en) * | 1985-06-06 | 1989-04-12 | Shell Internationale Researchmaatschappij B.V. | Epoxy resin preparation process |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
435 | Patent endorsed 'licences of right' on the date specified (sect. 35/1949) | ||
PE | Patent expired |